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U.S. Department of Health and Human Services

Class 2 Device Recall SOMATOM go.Top

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 Class 2 Device Recall SOMATOM go.Topsee related information
Date Initiated by FirmMay 28, 2019
Create DateJuly 02, 2019
Recall Status1 Terminated 3 on March 31, 2023
Recall NumberZ-1918-2019
Recall Event ID 83081
510(K)NumberK173632 
Product Classification System, x-ray, tomography, computed - Product Code JAK
ProductSOMATOM go.Top (Model #1161640), with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained physician as an aid in diagnosis. The images delivered by the system can be used by trained staff as an aid in diagnosis, treatment preparation and radiation therapy planning. This CT system can be used for low dose lung cancer screening in high risk populations. High risk populations are as defined by professional medical societies.
Code Information Serial Number: 119103 119090 119098 119086 119081 119115 119125 119145 119148 119119 119132 119123 119133 119084 119085 119088 119087 119141 119083 119143 119153 119122 119120 119093 119109 119111 119144 119152 119142 119147 
Recalling Firm/
Manufacturer		 Siemens Medical Solutions USA, Inc
40 Liberty Blvd
Malvern PA 19355-1418
For Additional Information ContactRebecca Tudor
610-219-4834
Manufacturer Reason
for Recall		The potential sporadic performance problems may result in scanning workflow interruptions and unexpected user notifications. This may cause a delay in diagnosis or patient scans.
FDA Determined
Cause 2		Software design
ActionUrgent Medical Device Correction letters dated 5/24/19 were sent to customers.
Quantity in Commerce30
DistributionUS Nationwide distributed in the states of AK, AL, AZ, CA, CO, CT, DC, FL, GA, IA, IL, IN, KS, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NY, OH, PA, SC, TX, VA, WA, WI, and Puerto Rico.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database510(K)s with Product Code = JAK
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